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10.1002/jmv.27117

http://scihub22266oqcxt.onion/10.1002/jmv.27117
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34061377!ä!34061377

suck abstract from ncbi


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pmid34061377      J+Med+Virol 2021 ; 93 (10): 5825-5832
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  • Inhibitory effect on SARS-CoV-2 infection of neferine by blocking Ca(2+) -dependent membrane fusion #MMPMID34061377
  • Yang Y; Yang P; Huang C; Wu Y; Zhou Z; Wang X; Wang S
  • J Med Virol 2021[Oct]; 93 (10): 5825-5832 PMID34061377show ga
  • The coronavirus disease 2019 (COVID-19) pandemic has focused attention on the need to develop effective therapeutics against the causative pathogen, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), and also against other pathogenic coronaviruses. In this study, we report on a kind of bisbenzylisoquinoline alkaloid, neferine, as a pan-coronavirus entry inhibitor. Neferine effectively protected HEK293/hACE2 and HuH7 cell lines from infection by different coronaviruses pseudovirus particles (SARS-CoV-2, SARS-CoV-2 [D614G, N501Y/D614G, 501Y.V1, 501Y.V2, 501Y.V3 variants], SARS-CoV, MERS-CoV) in vitro, with median effect concentration (EC(50) ) of 0.13-0.41 muM. Neferine blocked host calcium channels, thus inhibiting Ca(2+) -dependent membrane fusion and suppressing virus entry. This study provides experimental data to support the fact that neferine may be a promising lead for pan-coronaviruses therapeutic drug development.
  • |Antiviral Agents/*pharmacology[MESH]
  • |Benzylisoquinolines/*pharmacology[MESH]
  • |COVID-19/virology[MESH]
  • |Calcium/*metabolism[MESH]
  • |Cell Line[MESH]
  • |Coronavirus/drug effects/physiology[MESH]
  • |HEK293 Cells[MESH]
  • |Humans[MESH]
  • |Isoquinolines/pharmacology[MESH]
  • |Phenols/pharmacology[MESH]
  • |SARS-CoV-2/*drug effects/physiology[MESH]


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